THE CLINICAL SEVERITY OF HEMOGLOBIN S / BLACK ((A)γδβ)(0)-THALASSEMIA

Hemoglobin S/Black ((A)γδβ)(0)-thalassemia is a rare sickle cell disease (SCD) variant. Based on limited descriptions in the literature, the disease is reported as a mild microcytic anemia with an uncomplicated course. We report the clinical and laboratory data of nine patients whose diagnoses were...

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Bibliographic Details
Published in:Pediatr Blood Cancer
Main Authors: Cancio, Maria I., Aygun, Banu, Chui, David H. K., Rothman, Jennifer A., Scott, J. Paul, Estepp, Jeremie H., Hankins, Jane S.
Format: Artigo
Language:Inglês
Published: 2017
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6615052/
https://ncbi.nlm.nih.gov/pubmed/28453928
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pbc.26596
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